Canonical Allele Identifier: CA414793129
Gene: MT-CO2 HGNC NCBI

Linked Data

dbSNP Id: rs2068704546
MyVariant Identifiers: chrMT:g.7646A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7646A>G , J01415.2:m.7646A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.61A>G ENSP00000354876.1:p.Ile21Val
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